- 1Winclove Probiotics, Amsterdam, Netherlands
- 2Division of Human Nutrition, Wageningen University, Wageningen, Netherlands
- 3Department of Neurology, Gelderse Vallei Hospital, Ede, Netherlands
- 4NijBarrahus Fertility Center, Wolvega, Netherlands
- 5Department of Gastroenterology and Hepatology, Gelderse Vallei Hospital, Ede, Netherlands
Recent studies suggest that migraine may be associated with gastrointestinal (GI) disorders, including irritable bowel syndrome (IBS), inflammatory bowel syndrome, and celiac disease. Here, an overview of the associations between migraine and GI disorders is presented, as well as possible mechanistic links and clinical implications. People who regularly experience GI symptoms have a higher prevalence of headaches, with a stronger association with increasing headache frequency. Children with a mother with a history of migraine are more likely to have infantile colic. Children with migraine are more likely to have experienced infantile colic compared to controls. Several studies demonstrated significant associations between migraine and celiac disease, inflammatory bowel disease, and IBS. Possible underlying mechanisms of migraine and GI diseases could be increased gut permeability and inflammation. Therefore, it would be worthwhile to investigate these mechanisms further in migraine patients. These mechanisms also give a rationale to investigate the effects of the use of pre- and probiotics in migraine patients.
Introduction
Migraine is a common headache disorder with a lifetime prevalence of 13% in men and 33% in women (1). There are ictal (migraine attack) and interictal periods. Migraine is a highly disabling disease with high personal and social costs (2). Migraine can be considered as a complex neurogenic inflammatory disorder (3–5) but the pathophysiology is still not fully understood (6). It is a disease of the brain, possibly of the brainstem and is associated with increased synthesis and release of calcitonin gene related peptide (CGRP). A migraine attack can be blocked with CGRP antagonists (3, 7, 8). The actual pain is generated by nociceptors of trigeminal nerve endings in the dura. Low serotonin levels may sensitize the nociceptors of trigeminal neurons (9). Existing data support that serotonin is low interictal but increased ictally in migraineurs (10, 11). Ictally serotonin agonist, like triptans and ergotamins, which decrease serotonin are associated with relief of acute pain (7–9). In contrast tricyclic antidepressants and selective serotonin and noradrenaline reuptake inhibitors, which are associated with increases in serotonin, are utilized for migraine prevention (11). Migraine attacks can be triggered by intrinsic cerebral factors (CGRP release), nitric oxide like tri-nitroglycerine, corticotrophin releasing hormone (stress), pro-inflammatory cytokines, and degranulation of mast cells located in the dura (1, 3, 8). Migraine has a genetic background, but the concordance in monozygotic twins is only 20%, indicating the importance of environmental factors in getting the disease (12).
An environmental factor that may play an important role is the gut microbiota. The number of bacteria in the human gut outnumbers the human cells by approximately 10:1 (13). Due to recent technical developments, studies of the gut microbiota are no longer dependent on culture techniques, but use high-throughput sequencing techniques to investigate the intestinal bacterial species. Over 25 different diseases are currently associated with alterations in the composition of the gut microbiota. At the moment, most attention has been given to inflammatory bowel diseases (IBDs), allergy, diabetes, and obesity (14). Besides gastrointestinal (GI) diseases, the gut microbiota as an independent factor can also contribute to systemic diseases. This can be caused by the migration of stimulated immune cells, by systemic diffusion of microbial products or metabolites, or by bacterial translocation as a result of decreased intestinal barrier function (15).
The brain and the GI tract are strongly connected via neural, endocrine, and immune pathways (16–18). The communication occurs in two directions, not only from the brain to the gut but also the other way around. This recent finding on the role of the gut microbiota in the gut-brain axis suggests that the gut microbiota can be associated with brain functions and neurological diseases like migraine. In this review, associations between migraine and GI diseases are studied and possible therapeutic consequences are hypothesized.
Headache and Gastrointestinal Symptoms
Not all observational studies are restricted to migraine. The HEAD-hunt study, for example, looked at the relationship between GI symptoms and headache, including migraine (19). The study was a questionnaire-based cross-sectional study among more than 51,000 inhabitants of a county in Norway. The study showed a higher prevalence of headaches among people who regularly experience GI symptoms compared to the control group without GI complaints. The association between headache and GI complaints increased with increasing headache frequency. All the GI complaints were as common among persons with non-migrainous headache as among migraine patients. So both migraine and other types of headaches are more common in people with GI complaints.
Migraine and Gastroparesis
Gastroparesis is a chronic disorder manifested by delayed emptying of the stomach. Gastroparesis is a relatively common complication of diabetes. In a population of patients with symptoms of diabetic gastroparesis, the patients with cyclic symptom patterns had a higher incidence of migraine headaches (47 vs. 20%, p = 0.02) compared to patients without cyclic vomiting pattern (20). Migraine attacks are associated with delayed gastric emptying (21). This migraine-associated gastroparesis is a problem for the treatment of the migraine with oral medicines, like oral triptans (22). Initially, delayed gastric emptying was found during migraine attacks, now there are also indications that in the interictal periods migraine patients have delayed gastric emptying. However, the studies done so far have been small and inconsistent in their results (23, 24), so further research in this topic is warranted.
Migraine and Colic
Infantile colic is a common cause of inconsolable crying during the first months of life. It is defined according to criteria by Wessel as crying and fussing for more than 3 h per day, more than 3 days a week, and for more than 3 weeks in an otherwise healthy and well-fed infant (25). It affects many infants, with incidence rates ranging from 5 to 19% (26). Infantile colic might be caused by abdominal pain, although other causes cannot be excluded. A few studies have used probiotics to treat or prevent colic, with variable effects (27, 28). Colic has also been suggested as an early life expression of migraine, as in a group of 154 infant–mother pairs the children with a mother with a history of migraine (28 in total) were 2.6 times as likely to have colic as infants without maternal history of migraine (29). Recently, it has been shown that infants with abdominal colic have a lower intestinal microbiota diversity and stability compared to control infants in the first weeks of life (30). Moreover, children with migraine are more likely to have experienced infantile colic compared with controls (OR ranging from 1.6 to 6.6 between different studies) (31–33). Although long-term prospective studies have not yet been performed, these different studies indicate the existence of an association between migraine and infantile colic.
Migraine and Irritable Bowel Syndrome
Irritable bowel syndrome (IBS) is a functional bowel disorder characterized by abdominal pain, bloating, discomfort, and marked changes in bowel habits as described in the ROME III criteria (34). The exact pathophysiology of IBS is not understood yet. IBS and migraine are both 2–3 times more prevalent in women than in men (1, 35–37). IBS has been shown to be a disorder with an increased intestinal permeability and this permeability increases with more severe IBS symptoms (38).
A study among approximately 125,000 IBS patients, identified in a large national health insurance database, found a prevalence of migraine of 60 per 1000 against 22 per 1000 in a control population from the same database (39). After correction for gender and age, and stratification of the mean monthly total medical cost, the odds for being diagnosed with migraine were 60% higher for people in the IBS cohort compared to people in the non-IBS cohort (39). Also other studies with smaller sample sizes indicated that 25–50% of IBS subjects had migraine, whereas it was only 4–19% in controls (40, 41). A meta-analysis showed that overall IBS patients are at risk to have coexisting headache with an estimated OR of 2.7 (CI 2.3–3.1) (42). Although no distinction between headache and migraine was made in this study, this suggests higher prevalence of migraine in IBS patients.
A study in Korean migraine patients revealed high numbers of functional GI symptoms in migraine patients, of which IBS related symptoms were the most common (43). Unfortunately, these numbers were not compared with control subjects, also in the total population a large percentage of the people fulfill the Rome III criteria for IBS.
Experimental evidence for an association between IBS and migraine comes from a study in which an IgG-based elimination diet was given to migraine patients with IBS. Twenty-one patients were included in the double blind, randomized, controlled, cross-over clinical trial with usual diet, elimination diet, and provocation diet (44). Compared with baseline, the elimination diet was associated with a significant reduction in migraine attack count, duration and severity. Also a significant reduction in IBS complaints was observed, demonstrating an association between the two diseases.
Migraine and Celiac Disease
In patients who suffer from celiac disease, the immune system develops an autoimmune reaction against gliadin, the main protein in gluten. This inflammatory reaction is associated with intestinal damage, including dysfunction of the tight junctions resulting in an increased intestinal permeability (45–49). Celiac disease has been associated with migraine headache in case–control studies (50, 51). In one study, 14 out of 111 celiac disease patients (12.6%) reported migraine (50). The prevalence in controls was much lower, only 12 out of 211 controls (5.7%). In another study, migraine was present in 40 out of 188 celiac disease patients (21%), compared with 13 out of 178 controls (7%) (51). Conversely, there are also some indications that celiac disease is more frequent in migraine patients. One study showed that out of 90 adult migraine patients, 4 had celiac disease (4.4%), as opposed to only 1 out of the 236 controls (0.4%) (52). A second study in 72 pediatric patients with migraine showed four cases (5.5%) of elevated transglutaminase IgA antibodies. The transglutaminase IgA antibody level is a reliable indicator for the presence of celiac disease. Elevated transglutaminase IgA antibodies were found only in 1 out of the 147 controls (0.6%) (53). Another study among 87 pediatric migraine patients showed 1 child with celiac disease (1.1%), compared to 2 out of 543 controls (0.04%) (54). However, in another study no difference was found in the presence of celiac disease in 100 children with migraine and 1500 controls, being 2% for both groups (55). The association between migraine and celiac disease seems to be stronger in adult patients compared with children, although a direct comparison has not yet been investigated.
Only one study suggests that migraine in celiac disease patients may be relieved by treating celiac disease. Until now, the primary treatment for celiac disease is a gluten-free diet (56). The effect of a gluten-free diet was investigated in a small study with four patients with both migraine and celiac disease (52). In one patient migraine completely resolved. In the other three patients, a reduction in migraine frequency, duration, and intensity was reported. This suggests that a gluten-free diet used by celiac disease patients with migraine may give relief in both celiac disease and migraine. However, it should be noticed that only four patients were included in this study. Larger, well-designed studies to confirm these results are warranted.
Migraine and Inflammatory Bowel Disease
The two main forms of IBD are ulcerative colitis and Crohn’s disease (57). These diseases are characterized by defects in the barrier function of the intestinal epithelial layer and the mucosal immune system (46, 57). Factors that may trigger IBD are antibiotics, non-steroidal anti-inflammatory drugs, stress, and infection. All these factors decrease the mucosal barrier integrity, modulate the immune response, and change the luminal microenvironment, providing the susceptibility to inflammation (58).
Data about possible correlations between migraine and IBD are scarce. To our knowledge, only two studies investigated the comorbidity between migraine and IBD. In the first study done by Ford et al., 100 patients with Crohn’s disease or ulcerative colitis were selected from the Gastroenterology clinic at the University of North Carolina (59). The prevalence of migraine in the IBD patients was 30%. This prevalence rate is higher than the US population basal rate of 18.2% for females and 6.5% for males. In the Crohn’s disease patients migraine was more prevalent (36%) than in the ulcerative colitis patients (14.8%) (59). In the second study, 111 patients with IBD were questioned in a survey (51). Prevalence of self-reported migraine was higher in these subjects compared with controls (OR 2.66, 95% CI 1.08–6.54). No reports in the literature were found showing a reduction in migraine frequency or severity with improvements of inflammatory bowel symptoms.
Role for Gut Barrier Function in Migraine?
This overview of the literature suggests the existence of a rather strong relationship between GI disorders and migraine. One of the links between inflammatory diseases and migraine are enhanced pro-inflammatory immune responses (60). In intestinal disorders characterized by an increased intestinal permeability like IBS, IBD, and celiac disease enhanced pro-inflammatory immune responses have been reported (48, 61, 62). Enhanced levels of pro-inflammatory cytokines like tumor necrosis factor alpha and interleukin 1β in serum of migraine patients have been found during migraine attacks (63). These cytokines can act on the nociceptors of the trigeminal nerve, causing migraine. Also statistical significant associations have been reported between migraine and a wide range of inflammatory disorders like asthma, obesity, metabolic syndrome, allergies, and GI diseases (4, 5, 64–70). A strong trigger of pro-inflammatory immune responses is the leakage of lipopolysaccharides (LPS) from the intestinal lumen into the circulation. Enhanced levels of LPS can enter the circulation when the intestinal permeability is increased (leaky gut, Figure 1). Depending on genetic susceptibility, pro-inflammatory responses can occur in different parts of the body, e.g., in case of migraine on the nociceptors of the trigeminal nerve.
Gut permeability and inflammation are bidirectional related, increased permeability can cause inflammation, but inflammation can also cause increased gut permeability (71). An increased gut permeability, and thereby increased translocation of LPS can be caused by multiple factors, like medicines, exercise, mast cell activation, high fat diet, stress, etc. (72). The most used method to measure epithelial barrier function is with the lactulose/mannitol test. Mannitol is transported via the transcellular pathway whereas lactulose is absorbed through the paracellular pathway. In case of increased permeability, more lactulose passes the barrier and eventually ends up in the urine. Therefore, an increase in intestinal permeability is characterized by an increased ratio of lactulose/mannitol (38, 73). It can be hypothesized that reduction of the permeability of the intestine results in relief of migraine in the subgroup of patients in whom intestinal permeability plays a role in the disease. One specific group might be migraine patients with food allergies. Subjects with food allergies have an increased intestinal permeability compared with healthy controls (74). The role of food allergens in migraine is controversial, as evidence linking avoiding suspected food triggers with improvement in migraine is still limited (60). In the 1990s and the first 10 years of this century, there has been almost no interest in studying the relationship between migraine and diet (75). However, some recent studies suggest a role for IgG-mediated food allergy in migraine (44, 76), a hypothesis that warrants further investigations.
Treatment of Migraine with Probiotics?
Probiotics are living microorganisms that have beneficial effects on the health of the host (77). The most used probiotics are lactobacilli and bifidobacteria. Effects of probiotics are dependent on the used species and strain. Certain probiotics have shown to be effective in gut-related diseases, like infectious childhood diarrhea (78), the prevention of antibiotic-associated diarrhea (79, 80), and necrotizing enterocolitis in premature infants (81). For other clinical conditions, like atopic dermatitis, IBD, and IBS the results from clinical trials have been inconsistent (82, 83). This can be due to multiple factors like study population, duration, end-points, etc. An important variable are the different probiotic strains which are studied, making it difficult to draw conclusions about probiotics in general for these conditions. One of the possible working mechanisms of probiotics in the treatment of GI disorders is strengthening of the intestinal barrier. In vitro as well as in vivo, probiotics have shown to be able to improve the epithelial barrier function via different mechanisms (84, 85). Most mechanistic work has been done in cell culture systems or in animal models. In a randomized double-blind placebo-controlled cross-over study in healthy adults, probiotics were able to enhance the epithelial barrier by changing the location of the tight junctions proteins in the epithelial layer (86).
As probiotics may play a role in maintaining or improving gut barrier function in human beings, they can have a beneficial effect in migraine patients with an enhanced intestinal permeability as well. So far, no clinical randomized controlled trials have been published where migraine patients received nutritional therapy with probiotics. An uncontrolled study reported the effects of a combination of different probiotics (Lactobacillus acidophilus, Lactobacillus bulgaricus, Enterococcus faecium, and Bifidobacterium bifidum) with vitamins, minerals, micronutrients, and herbs in 40 migraine patients (87). At the onset of this study, the participants had a mean quality of life score of 38 [Medical Outcomes Trust Migraine Specific Quality of Life (MSQ) Questionnaire] and after 90 days of treatment their mean quality of life score was risen to 76. Sixty percent of the migraine patients experienced almost total relief from migraine attacks and they reported quality of life scores between 80 and 100.
Conclusion
Next to migraine, other brain diseases have been suggested to be associated with increased gut permeability, including depression, autism, and stress (15, 88–90). There is growing interest in the role of the gut microbiota in these brain diseases. In this review, a possible route via an increased intestinal permeability is suggested. There is an accumulation of studies on both migraine and GI disorders (Table 1). However, the findings of some (small) studies are not supported yet by other independent studies. Nevertheless placebo-controlled studies in migraine patients using treatments directed at increased intestinal permeability are warranted. We have recently started a study in which permeability of the gut is measured in migraine patients as well as in controls. We also started a double blind, placebo-controlled trial to investigate the effect of a probiotic product on gut permeability as well as severity and incidence of migraine attacks. Hopefully, these studies provide an answer to the question if gut permeability plays a role in migraine patients.
Conflict of Interest Statement
Saskia van Hemert is employee of Winclove Probiotics. Winclove produces, markets, and investigates probiotics. Other authors declare that they have no conflict of interest.
Abbreviations
CGRP, calcitonin gene related peptide; GI, gastrointestinal; IBD, inflammatory bowel disease; IBS, irritable bowel syndrome; LPS, lipopolysaccharides.
References
1. Launer LJ, Terwindt GM, Ferrari MD. The prevalence and characteristics of migraine in a population-based cohort: the GEM study. Neurology (1999) 53:537–42. doi: 10.1212/WNL.53.3.537
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
2. Bond DS, Roth J, Nash JM, Wing RR. Migraine and obesity: epidemiology, possible mechanisms and the potential role of weight loss treatment. Obes Rev (2011) 12:e362–71. doi:10.1111/j.1467-789X.2010.00791.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
3. Waeber C, Moskowitz MA. Migraine as an inflammatory disorder. Neurology (2005) 64:S9–15. doi:10.1212/WNL.64.10_suppl_2.S9
5. Monteith T, Goadsby P. Acute migraine therapy: new drugs and new approaches. Curr Treat Options Neurol (2011) 13:1–14. doi:10.1007/s11940-010-0105-6
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
6. Samsam M, Covenas R, Ahangari R, Yajeya J. Neuropeptides and other chemical mediators, and the role of anti-inflammatory drugs in primary headaches. AntiInflamm AntiAllergy Agents Med Chem (2010) 9:170–88. doi:10.2174/1871523011009030170
7. Sinclair SR, Kane SA, Van Der Schueren BJ, Xiao A, Willson KJ, Boyle J, et al. Inhibition of capsaicin-induced increase in dermal blood flow by the oral CGRP receptor antagonist, telcagepant (MK-0974). Br J Clin Pharmacol (2010) 69:15–22. doi:10.1111/j.1365-2125.2009.03543.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
8. Xanthos D, Gaderer S, Drdla R, Nuro E, Abramova A, Ellmeier W, et al. Central nervous system mast cells in peripheral inflammatory nociception. Mol Pain (2011) 7:42–58. doi:10.1186/1744-8069-7-42
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
9. Maneepak M, Le Grand S, Srikiatkhachorn A. Serotonin depletion increases nociception-evoked trigeminal NMDA receptor phosphorylation. Headache (2009) 49:375–82. doi:10.1111/j.1526-4610.2009.01341.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
10. Peterlin BL, Rapoport AM. Clinical pharmacology of the serotonin receptor agonist, zolmitriptan. Expert Opin Drug Metab Toxicol (2007) 3:899–911. doi:10.1517/17425255.3.6.899
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
11. Chai NC, Scher AI, Moghekar A, Bond DS, Peterlin BL. Obesity and headache: part I – a systematic review of the epidemiology of obesity and headache. Headache (2014) 54:219–34. doi:10.1111/head.12296
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
12. Russell M, Olesen J. Increased familial risk and evidence of genetic factor in migraine. BMJ (1995) 311:541–4. doi:10.1136/bmj.311.7004.541
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
13. Belkaid Y, Naik S. Compartmentalized and systemic control of tissue immunity by commensals. Nat Immunol (2013) 14:646–53. doi:10.1038/ni.2604
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
14. de Vos WM, de Vos EA. Role of the intestinal microbiome in health and disease: from correlation to causation. Nutr Rev (2012) 70(Suppl 1):S45–56. doi:10.1111/j.1753-4887.2012.00505.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
15. Wang Y, Kasper LH. The role of microbiome in central nervous system disorders. Brain Behav Immun (2014) 38C:1–12. doi:10.1016/j.bbi.2013.12.015
16. Collins SM, Surette M, Bercik P. The interplay between the intestinal microbiota and the brain. Nat Rev Microbiol (2012) 10:735–42. doi:10.1038/nrmicro2876
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
17. Cryan JF, Dinan TG. Mind-altering microorganisms: the impact of the gut microbiota on brain and behaviour. Nat Rev Neurosci (2012) 13:701–12. doi:10.1038/nrn3346
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
18. Chen X, D’Souza R, Hong ST. The role of gut microbiota in the gut-brain axis: current challenges and perspectives. Protein Cell (2013) 4:403–14. doi:10.1007/s13238-013-3017-x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
19. Aamodt A, Stovner L, Hagen K, Zwart J-A. Comorbidity of headache and gastrointestinal complaints. The head-HUNT study. Cephalalgia (2008) 28:144–51. doi:10.1111/j.1468-2982.2007.01486.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
20. Christensen CJ, Johnson WD, Abell TL. Patients with cyclic vomiting pattern and diabetic gastropathy have more migraines, abnormal electrogastrograms, and gastric emptying. Scand J Gastroenterol (2008) 43:1076–81. doi:10.1080/00365520802085411
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
21. Parkman HP. Migraine and gastroparesis from a gastroenterologist’s perspective. Headache (2013) 53(Suppl 1):4–10. doi:10.1111/head.12112
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
22. Newman LC. Why triptan treatment can fail: focus on gastrointestinal manifestations of migraine. Headache (2013) 53(Suppl 1):11–6. doi:10.1111/head.12111
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
23. Yalcin H, Okuyucu EE, Ucar E, Duman T, Yilmazer S. Changes in liquid emptying in migraine patients: diagnosed with liquid phase gastric emptying scintigraphy. Intern Med J (2012) 42:455–9. doi:10.1111/j.1445-5994.2012.02741.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
24. Aurora SK, Papapetropoulos S, Kori SH, Kedar A, Abell TL. Gastric stasis in migraineurs: etiology, characteristics, and clinical and therapeutic implications. Cephalalgia (2013) 33:408–15. doi:10.1177/0333102412473371
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
25. Wessel MA, Cobb JC, Jackson EB, Harris GS Jr, Detwiler AC. Paroxysmal fussing in infancy, sometimes called colic. Pediatrics (1954) 14:421–35.
26. Lucassen PL, Assendelft WJ, Van Eijk JT, Gubbels JW, Douwes AC, Van Geldrop WJ. Systematic review of the occurrence of infantile colic in the community. Arch Dis Child (2001) 84:398–403. doi:10.1136/adc.84.5.398
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
27. Sung V, Collett S, De Gooyer T, Hiscock H, Tang M, Wake M. Probiotics to Prevent or Treat Excessive Infant Crying: Systematic Review and Meta-analysis. JAMA Pediatr. (2013) 167:1150–7. doi:10.1001/jamapediatrics.2013.2572
28. Sung V, Hiscock H, Tang ML, Mensah FK, Nation ML, Satzke C, et al. Treating infant colic with the probiotic Lactobacillus reuteri: double blind, placebo controlled randomised trial. BMJ (2014) 348:g2107. doi:10.1136/bmj.g2107
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
29. Gelfand AA, Thomas KC, Goadsby PJ. Before the headache: infant colic as an early life expression of migraine. Neurology (2012) 79:1392–6. doi:10.1212/WNL.0b013e31826c1b7b
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
30. de Weerth C, Fuentes S, Puylaert P, De Vos WM. Intestinal microbiota of infants with colic: development and specific signatures. Pediatrics (2013) 131:e550–8. doi:10.1542/peds.2012-1449
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
31. Bruni O, Fabrizi P, Ottaviano S, Cortesi F, Giannotti F, Guidetti V. Prevalence of sleep disorders in childhood and adolescence with headache: a case-control study. Cephalalgia (1997) 17:492–8. doi:10.1046/j.1468-2982.1997.1704492.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
32. Jan MM, Al-Buhairi AR. Is infantile colic a migraine-related phenomenon? Clin Pediatr (Phila) (2001) 40:295–7. doi:10.1177/000992280104000512
33. Romanello S, Spiri D, Marcuzzi E, Zanin A, Boizeau P, Riviere S, et al. Association between childhood migraine and history of infantile colic. JAMA (2013) 309:1607–12. doi:10.1001/jama.2013.747
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
34. Talley NJ. Irritable bowel syndrome: definition, diagnosis and epidemiology. Baillieres Best Pract Res Clin Gastroenterol (1999) 13:371–84. doi:10.1053/bega.1999.0033
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
35. Muller-Lissner SA, Bollani S, Brummer RJ, Coremans G, Dapoigny M, Marshall JK, et al. Epidemiological aspects of irritable bowel syndrome in Europe and North America. Digestion (2001) 64:200–4. doi:10.1159/000048862
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
36. Berg J, Stovner LJ. Cost of migraine and other headaches in Europe. Eur J Neurol (2005) 1:59–62. doi:10.1111/j.1468-1331.2005.01192.x
37. Bixquert Jimenez M. Treatment of irritable bowel syndrome with probiotics. An etiopathogenic approach at last? Rev Esp Enferm Dig (2009) 101:553–64. doi:10.4321/S1130-01082009000800006
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
38. Zhou Q, Zhang B, Verne GN. Intestinal membrane permeability and hypersensitivity in the irritable bowel syndrome. Pain (2009) 146:41–6. doi:10.1016/j.pain.2009.06.017
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
39. Cole JA, Rothman KJ, Cabral HJ, Zhang Y, Farraye FA. Migraine, fibromyalgia, and depression among people with IBS: a prevalence study. BMC Gastroenterol (2006) 6:26. doi:10.1186/1471-230X-6-26
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
40. Jones R, Lydeard S. Irritable bowel syndrome in the general population. BMJ (1992) 304:87–90. doi:10.1136/bmj.304.6819.87
41. Vandvik PO, Wilhelmsen I, Ihlebaek C, Farup PG. Comorbidity of irritable bowel syndrome in general practice: a striking feature with clinical implications. Aliment Pharmacol Ther (2004) 20:1195–203. doi:10.1111/j.1365-2036.2004.02250.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
42. Chang FY, Lu CL. Irritable bowel syndrome and migraine: bystanders or partners? J Neurogastroenterol Motil (2013) 19:301–11. doi:10.5056/jnm.2013.19.3.301
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
43. Park JW, Cho YS, Lee SY, Kim ES, Cho H, Shin HE, et al. Concomitant functional gastrointestinal symptoms influence psychological status in Korean migraine patients. Gut Liver (2013) 7:668–74. doi:10.5009/gnl.2013.7.6.668
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
44. Aydinlar EI, Dikmen PY, Tiftikci A, Saruc M, Aksu M, Gunsoy HG, et al. IgG-based elimination diet in migraine plus irritable bowel syndrome. Headache (2013) 53:514–25. doi:10.1111/j.1526-4610.2012.02296.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
45. Ulevitch RJ, Tobias PS. Recognition of Gram-negative bacteria and endotoxin by the innate immune system. Curr Opin Immunol (1999) 11:19–22. doi:10.1016/S0952-7915(99)80004-1
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
46. Fasano A, Shea-Donohue T. Mechanisms of disease: the role of intestinal barrier function in the pathogenesis of gastrointestinal autoimmune diseases. Nat Clin Pract Gastroenterol Hepatol (2005) 2:416–22. doi:10.1038/ncpgasthep0259
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
47. Holtmeier W, Caspary WF. Celiac disease. Orphanet J Rare Dis (2006) 1:3. doi:10.1186/1750-1172-1-3
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
48. Schuppan D, Junker Y, Barisani D. Celiac disease: from pathogenesis to novel therapies. Gastroenterology (2009) 137:1912–33. doi:10.1053/j.gastro.2009.09.008
49. Visser J, Rozing J, Sapone A, Lammers K, Fasano A. Tight junctions, intestinal permeability, and autoimmunity: celiac disease and type 1 diabetes paradigms. Ann N Y Acad Sci (2009) 1165:195–205. doi:10.1111/j.1749-6632.2009.04037.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
50. Zelnik N, Pacht A, Obeid R, Lerner A. Range of neurologic disorders in patients with celiac disease. Pediatrics (2004) 113:1672–6. doi:10.1542/peds.113.6.1672
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
51. Dimitrova AK, Ungaro RC, Lebwohl B, Lewis SK, Tennyson CA, Green MW, et al. Prevalence of migraine in patients with celiac disease and inflammatory bowel disease. Headache (2013) 53:344–55. doi:10.1111/j.1526-4610.2012.02260.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
52. Gabrielli M, Cremonini F, Fiore G, Addolorato G, Padalino C, Candelli M, et al. Association between migraine and celiac disease: results from a preliminary case-control and therapeutic study. Am J Gastroenterol (2003) 98:625–9. doi:10.1111/j.1572-0241.2003.07300.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
53. Alehan F, Ozcay F, Erol I, Canan O, Cemil T. Increased risk for coeliac disease in paediatric patients with migraine. Cephalalgia (2008) 28:945–9. doi:10.1111/j.1468-2982.2008.01630.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
54. Borgna-Pignatti C, Fiumana E, Milani M, Calacoci M, Soriani S. Celiac disease in children with migraine. Pediatrics (2004) 114:1371. doi:10.1542/peds.2004-1337
55. Inaloo S, Dehghani SM, Farzadi F, Haghighat M, Imanieh MH. A comparative study of celiac disease in children with migraine headache and a normal control group. Turk J Gastroenterol (2011) 22:32–5. doi:10.4318/tjg.2011.0153
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
56. Rashtak S, Murray JA. Review article: coeliac disease, new approaches to therapy. Aliment Pharmacol Ther (2012) 35:768–81. doi:10.1111/j.1365-2036.2012.05013.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
57. Podolsky DK. Inflammatory bowel disease. N Engl J Med (2002) 347:417–29. doi:10.1056/NEJMra020831
58. Sartor RB. Mechanisms of disease: pathogenesis of Crohn’s disease and ulcerative colitis. Nat Clin Pract Gastroenterol Hepatol (2006) 3:390–407. doi:10.1038/ncpgasthep0528
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
59. Ford S, Finkel AG, Isaacs KL. Migraine in patients with inflammatory bowel disorders. J Clin Gastroenterol (2009) 43:499. doi:10.1097/MCG.0b013e318188be85
60. Finkel AG, Yerry JA, Mann JD. Dietary considerations in migraine management: does a consistent diet improve migraine? Curr Pain Headache Rep (2013) 17:373. doi:10.1007/s11916-013-0373-4
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
61. Rogler G, Andus T. Cytokines in inflammatory bowel disease. World J Surg (1998) 22:382–9. doi:10.1007/s002689900401
62. Liebregts T, Adam B, Bredack C, Roth A, Heinzel S, Lester S, et al. Immune activation in patients with irritable bowel syndrome. Gastroenterology (2007) 132:913–20. doi:10.1053/j.gastro.2007.01.046
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
63. Kemper RHA, Meijler WJ, Korf J, Ter Horst GJ. Migraine and function of the immune system: a meta-analysis of clinical literature published between 1966 and 1999. Cephalalgia (2001) 21:549–57. doi:10.1046/j.1468-2982.2001.00196.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
64. Téllez-Zenteno JF, Matijevic S, Wiebe S. Somatic comorbidity of epilepsy in the general population in Canada. Epilepsia (2005) 46:1955–62. doi:10.1111/j.1528-1167.2005.00344.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
65. Aamodt AH, Stovner LJ, Langhammer A, Hagen K, Zwart J-A. Is headache related to asthma, hay fever, and chronic bronchitis? The head-HUNT study. Headache (2007) 47:204–12. doi:10.1111/j.1526-4610.2006.00597.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
66. Kurth T, Schurks M, Logroscino G, Gaziano JM, Buring JE. Migraine, vascular risk, and cardiovascular events in women: prospective cohort study. BMJ (2008) 337:a636–44. doi:10.1136/bmj.a636
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
67. Bigal ME, Kurth T, Santanello N, Buse D, Golden W, Robbins M, et al. Migraine and cardiovascular disease: a population-based study. Neurology (2010) 74:628–35. doi:10.1212/WNL.0b013e3181d0cc8b
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
68. Peterlin BL, Rapoport AM, Kurth T. Migraine and obesity: epidemiology, mechanisms, and implications. Headache (2010) 50:631–48. doi:10.1111/j.1526-4610.2009.01554.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
69. de Tommaso M, Federici A, Serpino C, Vecchio E, Franco G, Sardaro M, et al. Clinical features of headache patients with fibromyalgia comorbidity. J Headache Pain (2011) 12:629–38. doi:10.1007/s10194-011-0377-6
70. Sachdev A, Marmura MJ. Metabolic syndrome and migraine. Front Neurol (2012) 3:161. doi:10.3389/fneur.2012.00161
71. Marchiando AM, Graham WV, Turner JR. Epithelial barriers in homeostasis and disease. Ann Rev Pathol (2010) 5:119–44. doi:10.1146/annurev.pathol.4.110807.092135
72. Farhadi A, Banan A, Fields J, Keshavarzian A. Intestinal barrier: an interface between health and disease. J Gastroenterol Hepatol (2003) 18:479–97. doi:10.1046/j.1440-1746.2003.03032.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
73. van Nieuwenhoven MA, Geerling BJ, Deutz NE, Brouns F, Brummer RJ. The sensitivity of the lactulose/rhamnose gut permeability test. Eur J Clin Invest (1999) 29:160–5. doi:10.1046/j.1365-2362.1999.00421.x
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
74. Perrier C, Corthesy B. Gut permeability and food allergies. Clin Exp Allergy (2011) 41:20–8. doi:10.1111/j.1365-2222.2010.03639.x
75. Pascual J, Oterino A. IgG-mediated allergy: a new mechanism for migraine attacks? Cephalalgia (2010) 30:777–9. doi:10.1177/0333102410364856
76. Alpay K, Ertas M, Orhan EK, Ustay DK, Lieners C, Baykan B. Diet restriction in migraine, based on IgG against foods: a clinical double-blind, randomised, cross-over trial. Cephalalgia (2010) 30:829–37. doi:10.1177/0333102410361404
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
77. FAO/WHO. Evaluation of health and nutritional properties of probiotics in food including powder milk with live lactic acid bacteria. Report of a Joint FAO/WHO Expert Consultation. Cordoba, Argentina (2001).
78. Allen SJ, Martinez EG, Gregorio GV, Dans LF. Probiotics for treating acute infectious diarrhoea. Cochrane Database Syst Rev (2010):CD003048. doi:10.1002/14651858.CD003048.pub3
79. Hempel S, Newberry SJ, Maher AR, Wang Z, Miles JN, Shanman R, et al. Probiotics for the prevention and treatment of antibiotic-associated diarrhea: a systematic review and meta-analysis. JAMA (2012) 307:1959–69. doi:10.1001/jama.2012.3507
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
80. Goldenberg JZ, Ma SS, Saxton JD, Martzen MR, Vandvik PO, Thorlund K, et al. Probiotics for the prevention of Clostridium difficile-associated diarrhea in adults and children. Cochrane Database Syst Rev (2013) 5:CD006095. doi:10.1002/14651858.CD006095.pub3
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
81. Alfaleh K, Anabrees J, Bassler D, Al-Kharfi T. Probiotics for prevention of necrotizing enterocolitis in preterm infants. Cochrane Database Syst Rev (2011):CD005496. doi:10.1002/14651858.CD005496.pub3
82. Floch MH, Walker WA, Madsen K, Sanders ME, Macfarlane GT, Flint HJ, et al. Recommendations for probiotic use-2011 update. J Clin Gastroenterol (2011) 45(Suppl):S168–71. doi:10.1097/MCG.0b013e318230928b
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
83. Sanders ME, Guarner F, Guerrant R, Holt PR, Quigley EM, Sartor RB, et al. An update on the use and investigation of probiotics in health and disease. Gut (2013) 62:787–96. doi:10.1136/gutjnl-2012-302504
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
84. Ohland CL, Macnaughton WK. Probiotic bacteria and intestinal epithelial barrier function. Am J Physiol Gastrointest Liver Physiol (2010) 298:G807–19. doi:10.1152/ajpgi.00243.2009
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
85. Van Hemert S, Verwer J, Schuetz B. Clinical studies evaluating effects of probiotics on parameters of intestinal barrier function. Adv Microbiol (2013) 3:212–21. doi:10.4236/aim.2013.32032
86. Karczewski J, Troost FJ, Konings I, Dekker J, Kleerebezem M, Brummer R-JM, et al. Regulation of human epithelial tight junction proteins by Lactobacillus plantarum in vivo and protective effects on the epithelial barrier. Am J Physiol (2010) 298:G851–9. doi:10.1152/ajpgi.00327.2009
Pubmed Abstract | Pubmed Full Text | CrossRef Full Text | Google Scholar
87. Sensenig J, Johnson M, Staverosky T. Treatment of migraine with targeted nutrition focused on improved assimilation and elimination. Altern Med Rev (2001) 6:488–94.
89. Maes M, Kubera M, Leunis JC. The gut-brain barrier in major depression: intestinal mucosal dysfunction with an increased transloca tion of LPS from gram negative enterobacteria (leaky gut) plays a role in the inflammatory pathophysiology of depression. Neuro Endocrinol Lett (2008) 29:117–24.
Keywords: celiac disease, colic, gastroparesis, migraine, inflammatory bowel disease, irritable bowel syndrome, leaky gut, probiotics
Citation: van Hemert S, Breedveld AC, Rovers JMP, Vermeiden JPW, Witteman BJM, Smits MG and de Roos NM (2014) Migraine associated with gastrointestinal disorders: review of the literature and clinical implications. Front. Neurol. 5:241. doi: 10.3389/fneur.2014.00241
Received: 09 September 2014; Accepted: 06 November 2014;
Published online: 21 November 2014.
Edited by:
Michael Marmura, Thomas Jefferson University, USAReviewed by:
Teshamae S. Monteith, University of Miami Miller School of Medicine, USAElcio J. Piovesan, Universidade Federal do Paraná, Brazil
Copyright: © 2014 van Hemert, Breedveld, Rovers, Vermeiden, Witteman, Smits and de Roos. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Saskia van Hemert, Winclove Probiotics, Hulstweg 11, Amsterdam 1032 LB, Netherlands e-mail: saskiavanhemert@winclove.nl